eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | ewing sarcoma |
| Comorbidity | C1261473|sarcoma |
| Sentences | 9 |
| PubMedID- 21826194 | Rhabdomyosarcoma, ewing sarcoma, osteosarcoma) and adult-type sarcomas which emerged in 30- to 49-year-old age group (e.g. |
| PubMedID- 24206917 | The first detected fusion genes in sarcoma were found in a patient with ewing sarcoma in 1983. this fusion, which is prevalent in 90% of these patients, forms via translocation between chromosomes 11 and 22, resulting in fusion of the ewing sarcoma breakpoint region 1 (ewsr1) gene to members of the e-twenty six (ets) gene family of transcription factor genes[26]–[28]. |
| PubMedID- 24805859 | Bcor-ccnb3 fusion transcripts resulting from an x-chromosomal paracentric inversion were recently identified in a series of unclassifiable soft tissue and bone sarcomas with ewing sarcoma-like morphology. |
| PubMedID- 25193511 | Medi-573 potently inhibited in vitro proliferation of sarcoma cell lines, with ewing sarcoma cell lines being the most sensitive. |
| PubMedID- 22971270 | Small cell osteosarcoma with ewing sarcoma breakpoint region 1 gene rearrangement detected by interphase fluorescence in situ hybridization. |
| PubMedID- 22374462 | In an analysis focussing on osteosarcoma, 2 of 4 ewing sarcoma samples were gd2-positive (heiner et al, 1987), and a primary ewing sarcoma passaged in nude mice was reported to express gd2 (cheung et al, 1987). |
| PubMedID- 24453659 | Osteosarcoma, ewing's sarcoma, and giant cell tumors of the bone frequently occur in the pelvis. |
| PubMedID- 20496272 | Cellular variant of extraskeletal myxoid chondrosarcoma with ewing's sarcoma-like areas: a diagnostic pitfall in core needle biopsy. |
| PubMedID- 26236597 | The final tissue diagnosis was small round cell sarcoma most consistent with atypical ewing sarcoma likely arising from the chest wall. |
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